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Increasingly Difficult to Accept Peripheral Neuropathy

Neuropathy | Last Active: Aug 10 12:43pm | Replies (233)

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I have had Idiopathic Small Fiber Neuropathy for almost 10 years. I retired from a major pharmaceutical company and I know how to do research and read and understand clinical trials. My industry has dropped the ball big time in researching neuropathy. The little research that has been done has been focused on pain relief. Very, very little research has been devoted to reversing and healing of neuropathy. It is a huge market in terms of sales potential but pharma companies seem to devote research dollars to eczema, plaque psoriasis, weight loss meds and migraines. I have been to several major medical institutions, including the Mayo Clinic in Rochester, MN. I spent an entire week there a few years ago and underwent an exhaustive round of testing. Every single test, to include bloodwork, came back normal.

There is one company from South Korea called Helixmith that has been researching a drug called Engensis. It is an injection in the calf and has been shown to REVERSE nerve damage from neuropathy! I have made many attempts to contact their U.S. office in California and nobody will take the time to answer my questions. The company has gone dark in terms of any new information coming out about Engensis. This leads me to believe that they have no intention of trying to get the drug submitted to the FDA for review. If they did, it would likely have been submitted last year.

There is a real possibility that no drug with real efficacy will come out for a very long time, if ever. It is extremely depressing. I don’t know what to tell people when they ask me what and when a real drug that will reverse neuropathy will ever come to market.

Neurologists realize that their hands are tied but deep down they know very little will help their neuropathy patients so they try all the drugs out there in the hopes something might just work. Please don’t fall for all the snake oil salesmen out there hawking their creams, machines and supplements because none of them have gone through rigorous clinical trials to check efficacy. They prey on our pain, depression and frustration that their crap might just help. God bless all of you suffering from neuropathy. It’s a long and painful journey.

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Replies to "I have had Idiopathic Small Fiber Neuropathy for almost 10 years. I retired from a major..."

Thank you brother. Amen

Good stuff. And I totally agree with you. I've been through the gamut of drugs as I've mentioned on here before. Although Cymbalta seems to work a little bit with the pain. Most of my success I believe came from reversing it a little bit not a great deal but enough to make it more comfortable, came from giving up sugar and processed food as much as possible if not 100 percent and going to whole food although it's expensive. Your comment was very interesting thanks for sharing.

It is so difficult to come to the conclusion that there isn’t much to do for the treatment of neuropathy. it is a sad thing to realize the supplement industry for neuropathy is becoming huge while there is so little actual research being done to find help for this disease.
I am troubled almost entirely by numbness from my knees down to my toes yes I have tried supplements and none of them have done any good
Has anybody read much about platelet rich plasma to be used for neuropathy?